Is Mg-stabilized amorphous calcium carbonate a homogeneous mixture of amorphous magnesium carbonate and amorphous calcium carbonate?

2016 ◽  
Vol 52 (77) ◽  
pp. 11527-11530 ◽  
Author(s):  
Sheng-Yu Yang ◽  
Hsun-Hui Chang ◽  
Cang-Jie Lin ◽  
Shing-Jong Huang ◽  
Jerry C. C. Chan

13C solid-state NMR data reveal that Mg stabilized amorphous calcium carbonate might be a homogeneous mixture of nanoclusters of amorphous calcium carbonate (ACC) and amorphous magnesium carbonate (AMC).

2008 ◽  
Vol 47 (17) ◽  
pp. 7874-7879 ◽  
Author(s):  
Holger Nebel ◽  
Markus Neumann ◽  
Christian Mayer ◽  
Matthias Epple

2006 ◽  
Vol 984 ◽  
Author(s):  
Paul Guerry ◽  
Donna L Carroll ◽  
Phillips N Gunawidjaja ◽  
Prodipta Bhattacharya ◽  
Daniela Carta ◽  
...  

AbstractTo understand amorphous and structurally disordered materials requires the application of a wide-range of advanced physical probe techniques and herein a combined methodology is outlined. The relatively short-range structural sensitivity of solid state NMR means that it is a core probe technique for characterizing such materials. The aspects of the solid state NMR contribution are emphasized here with examples given from a number of systems, with especial emphasis on the information available from 17O NMR in oxygen-containing materials. 17O NMR data for crystallization of pure sol-gel prepared oxides is compared, with new data presented from In2O3 and Sc2O3. Sol-gel formed oxide mixtures containing silica have been widely studied, but again the role and effect of the other added oxide varies widely. In a ternary ZrO2-TiO2-SiO2 silicate sol-gel the level of Q4 formation is dependent not only on the composition, as expected, but also the nature of the second added oxide. Sol-gel formed phosphates have been much less widely studied than silicates and some 31P NMR data from xerogel, sonogel and melt-quench glasses of the same composition are compared. The effect of small amounts of added antibacterial copper on phosphate glass networks is also explored.


2012 ◽  
Vol 23 (12) ◽  
pp. 1575-1585 ◽  
Author(s):  
Johannes Ihli ◽  
Yi-Yeoun Kim ◽  
Elizabeth H. Noel ◽  
Fiona C. Meldrum

2014 ◽  
Vol 60 (2-3) ◽  
pp. 85-90 ◽  
Author(s):  
ShengQi Xiang ◽  
Veniamin Chevelkov ◽  
Stefan Becker ◽  
Adam Lange

2001 ◽  
Vol 79 (10) ◽  
pp. 1505-1510 ◽  
Author(s):  
G W Buchanan ◽  
M F Rastegar ◽  
G PA Yap ◽  
A Moghimi ◽  
M Ghandi

Treatment of naphtho-9-crown-3 ether with FeCl3 and aqueous H2SO4 generates bis-naphtho-9-crown-3 ether in ca. 30% yield. This compound crystallizes in the monoclinic P21/n space group; a = 9.2004(9), b = 18.0868(17), and c = 13.2078(13) Å, β = 97.799(2)° and Z = 4. 1H and 13C NMR data have been obtained in solution, and the solid-state 13C NMR spectrum is included for comparison. A chemical shift range of ca. 12 ppm has been found for the oxygenated aliphatic carbons in the solid state, in contrast to the 3 ppm range in the solution 13C NMR spectrum. These results are discussed in terms of the torsional environments of the carbon sites in the crystal structure.Key words: crown ether, stereochemistry, oxidative dimerization.


Data in Brief ◽  
2017 ◽  
Vol 11 ◽  
pp. 136-146 ◽  
Author(s):  
Elenilson G. Alves Filho ◽  
Lorena M.A. Silva ◽  
Elizita M. Teofilo ◽  
Flemming H. Larsen ◽  
Edy S. de Brito

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